A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734923



Internal ID158589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102106161..102115105hg38UCSC Ensembl
chr3:101825005..101833949hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg388945
hg198945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441665
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734923
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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